
Grieshaber & Co.
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G.A.S./GRIESHABER AIR SYSTEM is an FDA 510(k)-cleared medical device (K860502) manufactured by Grieshaber & Co.. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 26, 1986. Regulation: 8.

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